The "Dynamic Tongue Contraction Technique" for Diagnosis of Soft Palate Cleft in Cases of Cleft Lip and Palate Sequence. [PDF]
Piura E +6 more
europepmc +1 more source
A New Model of Feeding Biomechanics Based on Tied‐Arch Principles
This new biomechanical model explains the major stress and strain patterns generated through the cranium during biting. The model proposes that the cranium resolves bite‐induced reaction forces through arcs of compressive stress that span the cranial structure between biting teeth and both jaw joints.
D. Rex Mitchell
wiley +1 more source
Oral Melanoma: A South American Collaborative Series of 21 Cases. [PDF]
de Arruda JAA +15 more
europepmc +1 more source
Congenital Insufficiency of Soft Palate [PDF]
openaire +2 more sources
Is Cone‐Beam CT Reliable for Apical Foramen Assessment? A Micro‐CT–Referenced Study
ABSTRACT This study evaluated the diagnostic accuracy of two cone‐beam CT (CBCT) dose protocols for identifying the number and trajectory deviation of apical foramina. Forty lower molars were scanned in Micro‐CT. Thereafter, all teeth were inserted into the mandible sockets and a titanium implant and an endodontically treated tooth with a cobalt ...
João Pedro de Lima +3 more
wiley +1 more source
Persistent Wnt/β-catenin signaling disables soft palatogenesis and palatal osteogenesis by inducing mesenchymal condensation. [PDF]
Wang B +9 more
europepmc +1 more source
Surgical Management of Non‐Allergic Rhinitis—An EAACI Task Force Position Paper
ABSTRACT Non‐allergic rhinitis is a frequent yet underdiagnosed cause of chronic nasal symptoms, including nasal congestion, rhinorrhoea, and upper airway hyperreactivity. Its pathophysiology involves neurogenic dysregulation, leading to excessive mucus production and vasodilation.
Marie Lundberg +18 more
wiley +1 more source
Two case reports of soft palate perforation as a complication of video laryngoscope-assisted tracheal intubation: mechanism analysis and preventative strategies. [PDF]
Huang HQ +5 more
europepmc +1 more source
Cousin Syndrome Due to TBX15 Gene Variants: Three Novel Cases and Review of the Literature
Cousin syndrome (MIM#260660) is a rare recognizable genetic disorder characterized by short stature, pelvi‐scapular dysplasia, and craniofacial dysmorphism due to biallelic pathogenic variants in the TBX15 gene. ABSTRACT Cousin syndrome (MIM#260660) is a rare genetic disorder characterized by short stature, pelvi‐scapular dysplasia and craniofacial ...
Wafaa Alharbi +6 more
wiley +1 more source
This study reports a female proband with a de novo 9q34.11 deletion affecting SET, who underwent a 28‐year diagnostic odyssey after an atypical Rett syndrome clinical diagnosis. Genomic and proteomics analyses confirmed SET haploinsufficiency, refining the critical 9q34.11 region, and supporting speech therapy benefits in improving meaningful ...
Angelo Condell +14 more
wiley +1 more source

